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8-12 years
Not Disclosed
10 July 29, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Clinical Scientist – Catalyst Clinical Research (Remote)

Job Summary:

Catalyst Clinical Research is seeking a Clinical Scientist to join its global team focused on oncology and multi-therapeutic studies. This fully remote role is ideal for an experienced professional with expertise in clinical data review, regulatory documentation, and scientific communication. You’ll collaborate closely with cross-functional teams to ensure high-integrity data for regulatory submissions and provide critical insights to support trial success.


Key Responsibilities:

  • Develop and execute clinical data review plans for assigned studies

  • Interpret safety and efficacy data using listings and visual analytics

  • Communicate data trends to Medical Monitors, Study Teams, and Clients

  • Support safety tracking and contribute to Safety Review Committees (SRC)

  • Generate data summary slides for DSMBs, SRCs, and internal reviews

  • Collaborate on CRF design, data queries, and clinical protocol inquiries

  • Participate in the review of regulatory documents (CSRs, INDs, IBs, etc.)

  • Assist in informal UAT testing of analytic dashboards

  • Mentor junior team members and contribute to team development

  • Contribute to scientific writing projects such as abstracts and posters

  • Serve as a clinical point of contact for internal teams and site staff


Required Skills & Qualifications:

  • Education: Advanced degree (PharmD, PhD, MSN, MPH preferred); OR Bachelor’s in life sciences/nursing with 12+ years of relevant experience

  • Experience: 8+ years in clinical research with strong data review background

  • Solid understanding of clinical development, GCP, ICH guidelines

  • Expertise in interpreting safety/efficacy data in oncology or complex trials

  • Familiarity with EDC systems and visual analytics platforms

  • Proficient in Microsoft Office Suite (Excel, Word, PowerPoint)

  • Strong communication, presentation, and scientific writing skills

  • Ability to manage multiple projects and shifting timelines

  • Proven leadership, mentoring, and problem-solving capabilities


Perks & Benefits:

  • Fully remote work flexibility

  • Opportunity to work with leading biotech sponsors and innovative trials

  • Supportive, collaborative, and expert team culture

  • Career growth within a fast-expanding global CRO

  • Exposure to high-impact oncology and multi-therapeutic programs

  • Competitive salary (based on qualifications and experience)

  • Travel opportunities to client meetings and scientific conferences


Company Overview:

Catalyst Clinical Research is a full-service global CRO delivering flexible, scalable clinical solutions to the biopharmaceutical and biotechnology sectors. With deep expertise in oncology and multi-therapeutic development, Catalyst leverages global talent, innovative platforms, and data-driven strategies to support breakthrough clinical studies.


Work Mode: Remote
Job Type: Full-Time
Experience Level: Senior (8–12+ years)


Apply Now

Are you ready to make a difference in clinical trials that impact patient lives? Join Catalyst Clinical Research as a Clinical Scientist and bring your clinical expertise to the forefront of innovation. Apply today to start your journey.